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1.
Zhongguo Dang Dai Er Ke Za Zhi ; 26(6): 619-624, 2024 Jun 15.
Article in Zh | MEDLINE | ID: mdl-38926379

ABSTRACT

OBJECTIVES: To assess the effectiveness and safety of prone positioning in the treatment of neonatal respiratory distress syndrome (NRDS) using invasive respiratory support. METHODS: A prospective study was conducted from June 2020 to September 2023 at Suining County People's Hospital, involving 77 preterm infants with gestational ages less than 35 weeks requiring invasive respiratory support for NRDS. The infants were randomly divided into a supine group (37 infants) and a prone group (40 infants). Infants in the prone group were ventilated in the prone position for 6 hours followed by 2 hours in the supine position, continuing in this cycle until weaning from the ventilator. The effectiveness and safety of the two approaches were compared. RESULTS: At 6 hours after enrollment, the prone group showed lower arterial blood carbon dioxide levels, inspired oxygen concentration, oxygenation index, rates of tracheal intubation bacterial colonization, and Neonatal Pain, Agitation and Sedation Scale scores compared to the supine group (P<0.05). There were no significant differences between the groups in terms of pH, arterial oxygen pressure, positive end-expiratory pressure, duration of mechanical ventilation, accidental extubation, ventilator-associated pneumonia, air leak syndrome, skin pressure sores, feeding intolerance, and grades II-IV intraventricular hemorrhage (P>0.05). CONCLUSIONS: Compared to supine positioning, prone ventilation effectively improves oxygenation, increases comfort, and reduces tracheal intubation bacterial colonization in neonates requiring mechanical ventilation for NRDS, without significantly increasing adverse reactions.


Subject(s)
Respiration, Artificial , Respiratory Distress Syndrome, Newborn , Humans , Prone Position , Infant, Newborn , Respiratory Distress Syndrome, Newborn/therapy , Male , Female , Prospective Studies , Respiration, Artificial/methods
2.
Sensors (Basel) ; 23(14)2023 Jul 12.
Article in English | MEDLINE | ID: mdl-37514618

ABSTRACT

This paper presents a novel motion control strategy based on model predictive control (MPC) for distributed drive electric vehicles (DDEVs), aiming to simultaneously control the longitudinal and lateral motion while considering efficiency and the driving feeling. Initially, we analyze the vehicle's dynamic model, considering the vehicle body and in-wheel motors, to establish the foundation for model predictive control. Subsequently, we propose a model predictive direct motion control (MPDMC) approach that utilizes a single CPU to directly follow the driver's commands by generating voltage references with a minimum cost function. The cost function of MPDMC is constructed, incorporating factors such as the longitudinal velocity, yaw rate, lateral displacement, and efficiency. We extensively analyze the weighting parameters of the cost function and introduce an optimization algorithm based on particle swarm optimization (PSO). This algorithm takes into account the aforementioned factors as well as the driving feeling, which is evaluated using a trained long short-term memory (LSTM) neural network. The LSTM network labels the response under different weighting parameters in various working conditions, i.e., "Nor", "Eco", and "Spt". Finally, we evaluate the performance of the optimized MPDMC through simulations conducted using MATLAB and CarSim software. Four typical scenarios are considered, and the results demonstrate that the optimized MPDMC outperforms the baseline methods, achieving the best performance.

3.
J Prosthet Dent ; 2023 May 26.
Article in English | MEDLINE | ID: mdl-37246097

ABSTRACT

The treatment of infants with trisomy 21 (TS21) with a myostimulation plate can improve their development and quality of life. The manufacture of these plates requires an accurate cast of the maxilla, and their efficacy relies on their stability and retention. As such, the quality of the impression is a determining factor. The lack of commercially available stock trays for infants with TS21 creates difficulties, including inadequate impression quality and the risk of inhaling impression material. The present technique simplifies impression making for infants with TS21 from 3 months of age to when their maxillary deciduous teeth erupt by using computer-aided design and computer-aided manufacturing (CAD-CAM) impression trays. Sixty-five stored gypsum maxillary casts from infants with TS21 that had been used to manufacture myostimulation plates were analyzed to select four differently sized representative casts for designing the impression trays. A CAD software program was used to digitally shape four sizes of the impression tray from the selected gypsum casts. Practitioners interested in this approach can download and export the standard tessellation language (STL) files using a quick response (QR) code. The impression trays should be manufactured with the stereolithography additive technique using biocompatible resin. This technique allows practitioners to make accurate maxilla impressions for infants with TS21 by manufacturing their own impression trays using the free-access STL files rather than the cumbersome conventional method.

4.
Am J Dent ; 35(2): 137-140, 2022 Jun.
Article in English | MEDLINE | ID: mdl-35798708

ABSTRACT

PURPOSE: This in vitro study evaluated the effect of sodium carbonate (Na2CO3) concentration on adhesion between two layers of irreversible hydrocolloid wash impression material. METHODS: The first layer of irreversible hydrocolloid was brushed with three concentrations (0.1, 0.7, or 7.0 wt.%) of Na2CO3. Irreversible hydrocolloid not brushed with Na2CO3 was used as a negative control. Adhesion between the two layers (bond strength and adhesion energy) was then evaluated using a traction test, and the fracture modes were identified. The results of traction test were analyzed with a one-way ANOVA followed by a Tukey post hoc test. Chi-square test was used for analyzed failure mode after testing (α= 0.05). RESULTS: The bond strength (0.034 ±0.005 MPa) and adhesion energy (60.240 ±12.817 J.m⁻ ²) of the 0.7% Na2CO3 group were significantly higher than those of the other groups (P< 0.05). The 0.7% Na2CO3 group displayed only cohesive failure (ײ= 16; P< 0.0001). CLINICAL SIGNIFICANCE: Conditioning the surface of the first layer of irreversible hydrocolloid with 0.7% sodium carbonate improved adhesion between the two layers and may help clinicians improve the quality of the preliminary impressions of removable complete dentures.


Subject(s)
Alginates , Dental Impression Materials , Alginates/chemistry , Carbonates , Colloids/chemistry , Dental Impression Materials/chemistry , Denture, Complete , Materials Testing
5.
Am J Dent ; 35(5): 251-254, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36261405

ABSTRACT

PURPOSE: To evaluate two agents for bonding denture bases and teeth manufactured either by stereolithography (SLA) or by the subtractive mixed technique. METHODS: Two types of cylinders [small for the tooth resin and large for the base resin) were designed using CAD software according to the ANSI/ADA 15-2008 (R2013)] specification. For SLA manufacturing, 30 small cylinders were shaped with Denture Teeth resin and 30 large cylinders with Denture Base resin. For the mixed technique, 30 large cylinders were manufactured by SLA with V-print dentbase resin, and 30 small cylinders were milled with a CediTEC DT disk. Half the specimens were bonded with liquid Denture Base resin and half with CediTEC Primer and Adhesive, according to the manufacturers' protocols. Shear bond strength was measured using a universal testing machine. The failure mode was noted for all the specimens. RESULTS: The shear bond strength values were not significantly different between the groups (P> 0.05). Specimens bonded with liquid Denture Base resin displayed cohesive failure (P> 0.05, ײ= 0). Of the specimens bonded with CediTEC Primer and Adhesive, cohesive failures were observed with five specimens manufactured with the SLA technique and one specimen manufactured with the mixed technique (P> 0.05, ײ= 3.33). The Chi-square test results were significant between groups with different bonding agents regardless of the technique used (P< 0.001). Within the limitations of the present study, even if the shear bond strength values were similar, the failure mode analysis suggests that the uncured liquid Denture Base resin may be more effective than the CediTEC Primer and Adhesive for bonding denture bases and teeth manufactured either by SLA or the mixed technique. CLINICAL SIGNIFICANCE: The present study suggests that the uncured liquid resin (Denture Base) used as a bonding agent and the denture base and tooth materials (V-Print and CediTEC DT) manufactured by SLA and the subtractive technique are clinically compatible.


Subject(s)
Dental Bonding , Denture Bases , Acrylic Resins/chemistry , Materials Testing , Dental Cements , Computer-Aided Design , Resins, Synthetic , Surface Properties , Dental Stress Analysis
6.
Molecules ; 27(12)2022 Jun 13.
Article in English | MEDLINE | ID: mdl-35744916

ABSTRACT

Textile scaffolds that are either 2D or 3D with tunable shapes and pore sizes can be made through textile processing (weaving, knitting, braiding, nonwovens) using microfilaments. However, these filaments lack nano-topographical features to improve bone cell adhesion and proliferation. Moreover, the diameter of such filaments should be higher than that used for classical textiles (10−30 µm) to enable adhesion and the efficient spreading of the osteoblast cell (>30 µm diameter). We report, for the first time, the fabrication of biodegradable nanostructured cylindrical PLLA (poly-L-Lactic acid) microfilaments of diameters 100 µm and 230 µm, using a single step melt-spinning process for straightforward integration of nano-scale ridge-like structures oriented in the fiber length direction. Appropriate drawing speed and temperature used during the filament spinning allowed for the creation of instabilities giving rise to nanofibrillar ridges, as observed by AFM (Atomic Force Microscopy). These micro-filaments were hydrophobic, and had reduced crystallinity and mechanical strength, but could still be processed into 2D/3D textile scaffolds of various shapes. Biological tests carried out on the woven scaffolds made from these nano-structured micro filaments showed excellent human bone cell MG 63 adhesion and proliferation, better than on smooth 30 µm- diameter fibers. Elongated filopodia of the osteoblast, intimately anchored to the nano-structured filaments, was observed. The filaments also induced in vitro osteogenic expression, as shown by the expression of osteocalcin and bone sialoprotein after 21 days of culture. This work deals with the fabrication of a new generation of nano-structured micro-filament for use as scaffolds of different shapes suited for bone cell engineering.


Subject(s)
Tissue Engineering , Tissue Scaffolds , Cell Adhesion , Cell Proliferation , Humans , Polyesters/pharmacology , Textiles , Tissue Scaffolds/chemistry
7.
J Oral Maxillofac Surg ; 79(8): 1650-1671, 2021 08.
Article in English | MEDLINE | ID: mdl-33775650

ABSTRACT

PURPOSE: Development of minimally invasive therapies for temporomandibular joint osteoarthritis (TMJOA) has focused on drug intra-articular injections to avoid the systemic adverse effects experienced when these substances are administered orally. Therefore, we performed a systematic review to answer the question "Which method of induction of a TMJOA-related pain model in rats leads to prolonged painful symptoms, allowing the best assessment of a sustained drug delivery system?" MATERIALS AND METHODS: Following the PRISMA guidelines, we searched MEDLINE for papers published from 1994 to July 2020 on a TMJ arthritis model using rats. We identified the means of pain induction and of nociception assessment. We assessed protocol bias using an adaptation of the QUADAS-2 tool. Animal selection, the reference standard method of pain assessment, applicability of a statistical assessment, and flow and timing were assessed. RESULTS: Of the 59 full papers we reviewed, 41 performed no pain assessment after the first 7 days following induction of the TMJ-related pain model. We eventually identified 18 long-term TMJOA-related pain models. Pain was induced by injection of toxic substances, most commonly Freund's complete adjuvant (50 µg per 50 µl), formalin at various concentrations, or monosodium iodoacetate (0,5 mg per 50 µl), into the TMJ, or by physical methods. Few studies reported data on pain after 21 days of follow-up. Heterogeneity of induction methods, pain assessment methods, and flow and timing biases precluded a meta-analysis. CONCLUSIONS: Given that pain is 1 of the main symptoms of TMJOA, experimental study protocols should include long-term pain assessment.


Subject(s)
Osteoarthritis , Temporomandibular Joint Disorders , Animals , Drug Delivery Systems , Injections, Intra-Articular , Osteoarthritis/drug therapy , Rats , Temporomandibular Joint , Temporomandibular Joint Disorders/drug therapy
8.
Mar Drugs ; 18(6)2020 Jun 02.
Article in English | MEDLINE | ID: mdl-32498225

ABSTRACT

Whey protein isolate (WPI) is a by-product from the production of cheese and Greek yoghurt comprising ß-lactoglobulin (ß-lg) (75%). Hydrogels can be produced from WPI solutions through heating; hydrogels can be sterilized by autoclaving. WPI hydrogels have shown cytocompatibility and ability to enhance proliferation and osteogenic differentiation of bone-forming cells. Hence, they have promise in the area of bone tissue regeneration. In contrast to commonly used ceramic minerals for bone regeneration, a major advantage of hydrogels is the ease of their modification by incorporating biologically active substances such as enzymes. Calcium carbonate (CaCO3) is the main inorganic component of the exoskeletons of marine invertebrates. Two polymorphs of CaCO3, calcite and aragonite, have shown the ability to promote bone regeneration. Other authors have reported that the addition of magnesium to inorganic phases has a beneficial effect on bone-forming cell growth. In this study, we employed a biomimetic, marine-inspired approach to mineralize WPI hydrogels with an inorganic phase consisting of CaCO3 (mainly calcite) and CaCO3 enriched with magnesium using the calcifying enzyme urease. The novelty of this study lies in both the enzymatic mineralization of WPI hydrogels and enrichment of the mineral with magnesium. Calcium was incorporated into the mineral formed to a greater extent than magnesium. Increasing the concentration of magnesium in the mineralization medium led to a reduction in the amount and crystallinity of the mineral formed. Biological studies revealed that mineralized and unmineralized hydrogels were not cytotoxic and promoted cell viability to comparable extents (approximately 74% of standard tissue culture polystyrene). The presence of magnesium in the mineral formed had no adverse effect on cell viability. In short, WPI hydrogels, both unmineralized and mineralized with CaCO3 and magnesium-enriched CaCO3, show potential as biomaterials for bone regeneration.


Subject(s)
Bone Regeneration/drug effects , Hydrogels/chemical synthesis , Hydrogels/pharmacology , Whey Proteins/pharmacology , Animals , Biocompatible Materials/metabolism , Calcium Carbonate , Cell Line , Cell Proliferation/drug effects , Cell Survival/drug effects , Hydrogels/chemistry , Magnesium , Mice , Minerals/metabolism , Osteoblasts/drug effects , Osteogenesis/drug effects , Whey Proteins/chemistry , Wound Healing/drug effects
9.
Am J Dent ; 33(6): 305-309, 2020 12.
Article in English | MEDLINE | ID: mdl-33439559

ABSTRACT

PURPOSE: To evaluate an injectable gel, recently proposed for the controlled release of "active oxygen" in periodontal pockets, compared to an antibiotic or an antiseptic gel, respectively. METHODS: The antimicrobial activity, injectability, texture properties, swelling and water uptake of the gels were studied. RESULTS: The "active oxygen" gel showed a bactericidal effect comparable to the two commercially available drug products (containing minocycline or chlorhexidine) on anaerobic periodontal pathogens and did not seem to affect aerobic strains. The gel was easy to inject and stable in an aqueous medium for several days. Texture analysis revealed potential gel fragility. CLINICAL SIGNIFICANCE: The investigated gel for local delivery of oxygen can help to selectively eradicate anaerobic bacteria associated with periodontitis and promote the recovery of a healthy-compatible oral flora.


Subject(s)
Anti-Infective Agents, Local , Periodontitis , Chlorhexidine/pharmacology , Gels , Humans , Periodontitis/drug therapy , Reactive Oxygen Species
10.
Molecules ; 24(6)2019 Mar 14.
Article in English | MEDLINE | ID: mdl-30875854

ABSTRACT

New anti-infective agents are urgently needed to fight microbial resistance. Methicillin-resistant Staphylococcus aureus (MRSA) strains are particularly responsible for complicated pathologies that are difficult to treat due to their virulence and the formation of persistent biofilms forming a complex protecting shell. Parasitic infections caused by Trypanosoma brucei and Leishmania mexicana are also of global concern, because of the mortality due to the low number of safe and effective treatments. Female inflorescences of hop produce specialized metabolites known for their antimicrobial effects but underexploited to fight against drug-resistant microorganisms. In this study, we assessed the antimicrobial potential of phenolic compounds against MRSA clinical isolates, T. brucei and L. mexicana. By fractionation process, we purified the major prenylated chalcones and acylphloroglucinols, which were quantified by UHPLC-UV in different plant parts, showing their higher content in the active flowers extract. Their potent antibacterial action (MIC < 1 µg/mL for the most active compound) was demonstrated against MRSA strains, through kill curves, post-antibiotic effects, anti-biofilm assays and synergy studies with antibiotics. An antiparasitic activity was also shown for some purified compounds, particularly on T. brucei (IC50 < 1 to 11 µg/mL). Their cytotoxic activity was assessed both on cancer and non-cancer human cell lines.


Subject(s)
Anti-Infective Agents/chemistry , Biological Products/chemistry , Humulus/chemistry , Methicillin-Resistant Staphylococcus aureus/drug effects , Anti-Infective Agents/pharmacology , Bacterial Infections/drug therapy , Bacterial Infections/microbiology , Biofilms/drug effects , Biological Products/pharmacology , Humans , Leishmania mexicana/drug effects , Leishmania mexicana/pathogenicity , Methicillin-Resistant Staphylococcus aureus/chemistry , Methicillin-Resistant Staphylococcus aureus/pathogenicity , Microbial Sensitivity Tests , Parasitic Diseases/drug therapy , Parasitic Diseases/parasitology , Trypanosoma brucei brucei/drug effects , Trypanosoma brucei brucei/pathogenicity
11.
Mol Pharm ; 13(1): 125-33, 2016 Jan 04.
Article in English | MEDLINE | ID: mdl-26592866

ABSTRACT

Inkjet-printing technology was used to apply biodegradable and biocompatible polymeric coatings of poly(d,l-lactide) with the antiproliferative drugs simvastatin (SMV) and paclitaxel (PCX) on coronary metal stents. A piezoelectric dispenser applied coating patterns of very fine droplets (300 pL) and inkjet printing was optimized to develop uniform, accurate and reproducible coatings of high yields on the stent strut. The drug loaded polymeric coatings were assed by scanning electron microscopy (SEM), atomic force microscopy (AFM), and transition thermal microscopy (TTM) where a phase separation was observed for SMV/PLA layers while PCX showed a uniform distribution within the polymer layers. Cytocompatibility studies of PLA coatings showed excellent cell adhesion with no decrease of cell viability and proliferation. In vivo stent implantation studies showed significant intrastent restenosis (ISR) for PCX/PLA and PLA plain coatings similar to marketed Presillion (bare metal) and Cypher (drug eluting) stents. The investigation of several cytokine levels after 7 days of stent deployment showed no inflammatory response and hence no in vivo cytotoxicity related to PLA coatings. Inkjet printing can be employed as a robust coating technology for the development of drug eluting stents compared to the current conventional approaches.


Subject(s)
Drug-Eluting Stents , Paclitaxel/chemistry , Coated Materials, Biocompatible/chemistry , Cytokines/chemistry , Drug Delivery Systems/methods , Microscopy, Atomic Force , Microscopy, Electron, Scanning , Polymers/chemistry
12.
Helicobacter ; 21(2): 158-62, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26347248

ABSTRACT

INTRODUCTION: Very limited data are available on the Helicobacter pylori infection among the population of interior Borneo. We aimed to investigate the H. pylori infection rate among an endoscoped interior Borneo population and to report the differences between the infected and noninfected patients. METHODS: We retrospectively analyzed the data of the rapid urease test (RUT) records in Endoscopy Unit Hospital Keningau from January 2009 to May 2014. Student's t-test, chi-square test or Fisher's exact test were used accordingly. Multiple logistic regression analysis was used to identify independent risk factors for H. pylori infection. Birth cohort was analyzed against H. pylori infection rate with chi-square test. RESULTS: Overall, there were 215 of 774 (27.8%) positive RUTs. Patients with H. pylori infection were younger (47.66 ± 14.93 vs 50.50 ± 15.02 years, p = .019), more likely to be female (OR = 1.54, 95% CI 1.12-2.13, p = .008) and originated from the Pensiangan district (OR = 1.63, 95% CI 1.01-2.64, p = .047). Chinese patients were less likely infected with H. pylori (OR = 0.36, 95% CI 0.16-0.80, p = .013). Birth cohort was significantly associated with H. pylori infection rate (χ(2) (7) = 14.71, p = .040) with an increasing trend of H. pylori infection rate in patients born later (χ(2) (1) = 5.26, p = .022). CONCLUSION: The overall H. pylori infection rate in this population was unexpectedly low. Accordingly, it may be a recent arrival in this community. Gender, age, dietary practice, socioeconomic status, and ethnicity were among the factors associated with H. pylori infection.


Subject(s)
Helicobacter Infections/epidemiology , Helicobacter pylori/isolation & purification , Adult , Aged , Borneo/epidemiology , Endoscopy, Gastrointestinal , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors , Urease/analysis
13.
Antimicrob Agents Chemother ; 59(2): 930-4, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25421476

ABSTRACT

Peripheral intravenous therapy is frequently used in routine hospital practice and, due to various factors, its most common side effect is phlebitis. The infusion of vancomycin is particularly associated with phlebitis despite its widespread use. French guidelines recommend central intravenous infusion for high concentrations of vancomycin, but peripheral intravenous therapy is often preferred in intensive care units. Methods of vancomycin infusion are either intermittent infusion or continuous infusion. A comparison of these methods under in vitro conditions simulating clinical use could result in better infusion efficacy. Human umbilical vein endothelial cells (HUVECs) were therefore challenged with clinical doses of vancomycin over a 24- to 72-h period using these infusion methods. Cell death was measured with the alamarBlue test. Concentration-dependent and time-dependent vancomycin toxicity on HUVECs was noted with a 50% lethal dose at 5 mg/ml after 24 h, reaching 2.5 mg/ml after 72 h of infusion, simulating long-term infusion. This toxicity does not seem to be induced by acidic pH. In comparing infusion methods, we observed that continuous infusion induced greater cell toxicity than intermittent infusion at doses higher than 1 g/day. The increasing use of vancomycin means that new guidelines are required to avoid phlebitis. If peripheral intravenous therapy is used to reduce infusion time, along with intermittent infusion, vein irritation and localized phlebitis may be reduced. Further studies have to be carried out to explore the causes of vancomycin endothelial toxicity.


Subject(s)
Anti-Bacterial Agents/pharmacology , Endothelial Cells/drug effects , Vancomycin/pharmacology , Cell Death/drug effects , Human Umbilical Vein Endothelial Cells , Humans
14.
Antimicrob Agents Chemother ; 59(8): 4901-6, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26055373

ABSTRACT

French guidelines recommend central intravenous (i.v.) infusion for high concentrations of vancomycin, but peripheral intravenous (p.i.v.) infusion is often preferred in intensive care units. Vancomycin infusion has been implicated in cases of phlebitis, with endothelial toxicity depending on the drug concentration and the duration of the infusion. Vancomycin is frequently infused in combination with other i.v. antibiotics through the same administrative Y site, but the local toxicity of such combinations has been poorly evaluated. Such an assessment could improve vancomycin infusion procedures in hospitals. Human umbilical vein endothelial cells (HUVEC) were challenged with clinical doses of vancomycin over 24 h with or without other i.v. antibiotics. Cell death was measured with the alamarBlue test. We observed an excess cellular death rate without any synergistic effect but dependent on the numbers of combined infusions when vancomycin and erythromycin or gentamicin were infused through the same Y site. Incompatibility between vancomycin and piperacillin-tazobactam was not observed in our study, and rinsing the cells between the two antibiotic infusions did not reduce endothelial toxicity. No endothelial toxicity of imipenem-cilastatin was observed when combined with vancomycin. p.i.v. vancomycin infusion in combination with other medications requires new recommendations to prevent phlebitis, including limiting coinfusion on the same line, reducing the infusion rate, and choosing an intermittent infusion method. Further studies need to be carried out to explore other drug combinations in long-term vancomycin p.i.v. therapy so as to gain insight into the mechanisms of drug incompatibility under multidrug infusion conditions.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/adverse effects , Drug Therapy, Combination/adverse effects , Human Umbilical Vein Endothelial Cells/drug effects , Vancomycin/administration & dosage , Vancomycin/adverse effects , Cell Death/drug effects , Cells, Cultured , Cilastatin/administration & dosage , Cilastatin/adverse effects , Cilastatin, Imipenem Drug Combination , Drug Combinations , Erythromycin/administration & dosage , Erythromycin/adverse effects , Gentamicins/administration & dosage , Gentamicins/adverse effects , Humans , Imipenem/administration & dosage , Imipenem/adverse effects , Infusions, Intravenous/methods
15.
Invest New Drugs ; 33(1): 159-68, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25294187

ABSTRACT

PURPOSE: This phase I study evaluated the safety, tolerability, maximum tolerated dose (MTD), and recommended phase II dose (RP2D) of tivantinib combined with sorafenib in patients with advanced solid tumors. MATERIALS AND METHODS: A standard 3 + 3 dose escalation design was used. At the RP2D, expansion cohorts in 5 tumor types could be enrolled. Pharmacogenetic and pharmacodynamic analysis were performed. RESULTS: Eighty-seven patients received the study treatment. The combination had no unexpected toxicities. The most common treatment-related adverse events (AE) were rash (40 %), diarrhea (38 %), and anorexia (33 %). The RP2D was tivantinib 360 mg BID and sorafenib 400 mg BID for all cancer histologies, except in hepatocellular carcinoma (HCC) patients tivantinib was 240 mg BID plus sorafenib 400 mg BID. The overall response rate was 12 % in all patients, 26 % in melanoma, 15 % in renal cell carcinoma (RCC), 10 % in HCC, and 0 % in other patients. Disease control rate (CR, PR and SD ≥8 weeks) was 58 % in all patients, 90 % in RCC, 65 % in HCC, 63 % in melanoma, 40 % in breast cancer, and 8 % in NSCLC patients. CONCLUSIONS: The combination treatment could be administered at full standard single-agent doses in all patients except those with HCC, where tivantinib was lowered to 240 mg BID. Preliminary evidence of anticancer activity was observed in patients with RCC, HCC, and melanoma, including patients refractory to sorafenib and/or other anti-VEGF pathway therapies. The combination treatment has therapeutic potential in treating a variety of solid tumors.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Neoplasms/drug therapy , Adult , Aged , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/pharmacokinetics , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Cytochrome P-450 CYP2C19/genetics , Female , Humans , Male , Maximum Tolerated Dose , Middle Aged , Neoplasms/genetics , Neoplasms/metabolism , Niacinamide/administration & dosage , Niacinamide/adverse effects , Niacinamide/analogs & derivatives , Niacinamide/pharmacokinetics , Niacinamide/pharmacology , Phenylurea Compounds/administration & dosage , Phenylurea Compounds/adverse effects , Phenylurea Compounds/pharmacokinetics , Phenylurea Compounds/pharmacology , Polymorphism, Genetic , Proto-Oncogene Proteins c-met/metabolism , Pyrrolidinones/administration & dosage , Pyrrolidinones/adverse effects , Pyrrolidinones/pharmacokinetics , Pyrrolidinones/pharmacology , Quinolines/administration & dosage , Quinolines/adverse effects , Quinolines/pharmacokinetics , Quinolines/pharmacology , Sorafenib , Treatment Outcome , Young Adult
16.
World J Surg ; 44(10): 3322-3323, 2020 10.
Article in English | MEDLINE | ID: mdl-32524160
17.
Ann Vasc Surg ; 29(8): 1648-55, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26254604

ABSTRACT

BACKGROUND: In-stent restenosis (ISR) remains a major public health concern associated with an increased morbidity, mortality, and health-related costs. Drug-eluting stents (DES) have reduced ISR, but generate healing-related issues or hypersensitivity reactions, leading to an increased risk of late acute stent thrombosis. Assessments of new DES are based on animal models or in vitro release systems, which have several limitations. The role of flow and shear stress on endothelial cell and ISR has also been emphasized. The aim of this work was to design and first evaluate an original bioreactor, replicating ex vivo hemodynamic and biological conditions similar to human conditions, to further evaluate new DES. METHODS: This bioreactor was designed to study up to 6 stented arteries connected in bypass, immersed in a culture box, in which circulated a physiological systolo-diastolic resistive flow. Two centrifugal pumps drove the flow. The main pump generated pulsating flows by modulation of rotation velocity, and the second pump worked at constant rotation velocity, ensuring the counter pressure levels and backflows. The flow rate, the velocity profile, the arterial pressure, and the resistance of the flow were adjustable. The bioreactor was placed in an incubator to reproduce a biological environment. RESULTS: A first feasibility experience was performed over a 24-day period. Three rat aortic thoracic arteries were placed into the bioreactor, immersed in cell culture medium changed every 3 days, and with a circulating systolic and diastolic flux during the entire experimentation. There was no infection and no leak. At the end of the experimentation, a morphometric analysis was performed confirming the viability of the arteries. CONCLUSIONS: We designed and patented an original hemodynamic ex vivo model to further study new DES, as well as a wide range of vascular diseases and medical devices. This bioreactor will allow characterization of the velocity field and drug transfers within a stented artery with new functionalized DES, with experimental means not available in vivo. Another major benefit will be the reduction of animal experimentation and the opportunity to test new DES or other vascular therapeutics in human tissues (human infrapopliteal or coronary arteries collected during human donation).


Subject(s)
Bioreactors , Drug-Eluting Stents , Materials Testing , Models, Biological , Animals , Aorta , Humans , Prosthesis Design , Rats , Shear Strength , Vascular Resistance
18.
Am J Dent ; 28(2): 105-10, 2015 Apr.
Article in English | MEDLINE | ID: mdl-26087577

ABSTRACT

PURPOSE: To compare the effect of different treatments (heat capsule, ultrasound, and dual treatments) on the setting kinetics and maturation properties of a conventional GIC (EQUIA, GC) to that of standard setting. METHODS: The optimal durations of the heat and ultrasonic treatments were determined by monitoring changes in the COO-/COOH ratio, surface hardness, and temperature within the samples. The influence of optimal treatments on the maturation properties of the GIC (microhardness, and 3-point flexural strength) were assessed using GIC samples incubated in artificial saliva for 24 hours, 1 month, and 3 months. RESULTS: The optimal durations of the heat and ultrasonic treatments for accelerating setting were 5 minutes and 35 seconds, respectively. The dual treatment using the optimal conditions of the individual treatments further enhanced the setting kinetics. A temperature peak (49°C) within the GIC was detected during setting. Only the dual treatment increased the mechanical properties of the GIC after 24 hours compared to the control, while no significant difference was observed after 1 and 3 months.


Subject(s)
Glass Ionomer Cements/chemistry , Carbon Dioxide/analysis , Carbon Dioxide/chemistry , Carboxylic Acids/analysis , Carboxylic Acids/chemistry , Free Radicals/analysis , Free Radicals/chemistry , Glass Ionomer Cements/analysis , Hardness , Hot Temperature , Humans , Kinetics , Materials Testing , Pliability , Saliva, Artificial/chemistry , Stress, Mechanical , Time Factors , Ultrasonics
19.
Wei Sheng Yan Jiu ; 44(1): 77-81, 90, 2015 Jan.
Article in Zh | MEDLINE | ID: mdl-25958642

ABSTRACT

OBJECTIVE: To analyze the relationship between joint of heat and noise, and metabolic syndrome in a steel rolling factory workers. METHODS: A total of 590 steel workers were selected as subjects by cluster sampling method from workers of a steel factory. They were investigated by face to face way with the unified questionnaire which contents included personal information, occupational history, personal history, habits and other factors. Furthermore, height, weight, waist circumference and blood pressure were measured. Referring to the 2005 International Diabetes Federation (IDF) issued by the metabolic syndrome (MS) worldwide uniform definition combines waist diagnosis MS. A database was built by Epidata 3.0 software, and data was analyzed by SPSS 17.0. RESULTS: 571 steel workers were from 22 to 60 years, mean age (41.2 -7.9) years old. The prevalence of metabolic syndrome in steel workers was 17.9%. The prevalence of metabolic syndrome of those who exposed to high temperature was 18.8%, higher than that of those who did not expose to high temperature (5.3%), there was a statistically significant difference (P < 0.05). The prevalence of metabolic syndrome of those who exposed to noise was 20.6%, higher than that of those who did not exposed to noise (14.0%) (P < 0.05). After adjusting for the effects of confounding factors, the prevalence of MS those who exposed to high temperatures and noise is 1.118 times as high as that of those who did not exposed to high temperatures and noise. CONCLUSIONS: The combined effects of heat and noise is related to the increasing prevalence of MS of steel workers.


Subject(s)
Hot Temperature/adverse effects , Metabolic Syndrome/epidemiology , Metallurgy , Noise, Occupational/adverse effects , Occupational Exposure/adverse effects , Adult , Blood Pressure , Body Weight , Humans , Middle Aged , Prevalence , Steel , Waist Circumference , Young Adult
20.
Materials (Basel) ; 17(7)2024 Apr 02.
Article in English | MEDLINE | ID: mdl-38612144

ABSTRACT

This study investigated the effects of reheating temperature on the microstructure and mechanical properties of Cu-containing 440 MPa grade non-tempered ship plate steel. The mechanical properties test, thermodynamic simulation, optical microscopy, scanning electron microscopy, transmission electron microscopy, and other tests were performed. The results revealed that with increasing reheating temperature, the ferrite grain size of Cu-containing 440 MPa non-tempered ship plate steel increased. Also, with increasing reheating temperature, the size of copper particles and niobium-titanium composite precipitates in the original austenite decreased. Consequently, this led to a weakening of the pinning effect on the original austenite and an increase in the size of the transformed ferrite grains. Moreover, with increasing reheating temperature, the number of Cu precipitates in the test steel after air cooling and rolling increased, while the size of the precipitates decreased, thereby weakening the solid solution strengthening effect of Cu, and precipitation was enhanced. Additionally, as the reheating temperature increased, the tensile strength and yield strength of the air-cooled test steel after rolling increased, while the impact toughness decreased.

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